Weber Andrea Nicole, Trebach Joshua, Brenner Marielle A, Thomas Mary Margaret, Bormann Nicholas L
Department of Psychiatry, University of Iowa, Iowa City, IA, USA.
Department of Emergency Medicine, University of Iowa, Iowa City, IA, USA.
Subst Abuse Rehabil. 2024 Apr 10;15:59-71. doi: 10.2147/SAR.S433358. eCollection 2024.
Illicitly manufactured fentanyl (IMF) is a significant contributor to the increasing rates of overdose-related deaths. Its high potency and lipophilicity can complicate opioid withdrawal syndromes (OWS) and the subsequent management of opioid use disorder (OUD). This scoping review aimed to collate the current OWS management of study populations seeking treatment for OWS and/or OUD directly from an unregulated opioid supply, such as IMF. Therefore, the focus was on therapeutic interventions published between January 2010 and November 2023, overlapping with the period of increasing IMF exposure. A health science librarian conducted a systematic search on November 13, 2023. A total of 426 studies were screened, and 173 studies were reviewed at the full-text level. Forty-nine studies met the inclusion criteria. Buprenorphine and naltrexone were included in most studies with the goal of transitioning to a long-acting injectable version. Various augmenting agents were tested (buspirone, memantine, suvorexant, gabapentin, and pregabalin); however, the liberal use of adjunctive medication and shortened timelines to initiation had the most consistently positive results. Outside of FDA-approved medications for OUD, lofexidine, gabapentin, and suvorexant have limited evidence for augmenting opioid agonist initiation. Trials often have low retention rates, particularly when opioid agonist washout is required. Neurostimulation strategies were promising; however, they were developed and studied early. Precipitated withdrawal is a concern; however, the rates were low and adequately mitigated or managed with low- or high-dose buprenorphine induction. Maintenance treatment continues to be superior to detoxification without continued management. Shorter induction protocols allow patients to initiate evidence-based treatment more quickly, reducing the use of illicit or non-prescribed substances.
非法制造的芬太尼(IMF)是导致过量用药相关死亡人数不断上升的一个重要因素。其高效力和亲脂性会使阿片类药物戒断综合征(OWS)以及随后的阿片类药物使用障碍(OUD)管理变得复杂。本范围综述旨在整理目前针对直接从不受监管的阿片类药物供应(如IMF)中寻求OWS和/或OUD治疗的研究人群的OWS管理情况。因此,重点是2010年1月至2023年11月期间发表的治疗性干预措施,这一时期与IMF暴露增加的时间段重叠。一位健康科学图书馆员于2023年11月13日进行了系统检索。共筛选了426项研究,并对173项研究进行了全文审查。49项研究符合纳入标准。大多数研究都纳入了丁丙诺啡和纳曲酮,目标是过渡到长效注射剂型。测试了各种增效剂(丁螺环酮、美金刚、苏沃雷生、加巴喷丁和普瑞巴林);然而,辅助药物的大量使用和缩短开始治疗的时间线产生了最一致的积极结果。在FDA批准用于OUD的药物之外,洛非西定、加巴喷丁和苏沃雷生在增强阿片类激动剂启动方面的证据有限。试验的保留率往往较低,尤其是在需要停用阿片类激动剂时。神经刺激策略很有前景;然而,它们是早期开发和研究的。戒断反应是一个问题;然而,发生率较低,通过低剂量或高剂量丁丙诺啡诱导可得到充分缓解或控制。维持治疗仍然优于不进行持续管理的戒毒治疗。较短的诱导方案使患者能够更快地开始循证治疗,减少非法或非处方药物的使用。